[PDF] Top 20 A 3-year prognostic score for adults with cystic fibrosis
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A 3-year prognostic score for adults with cystic fibrosis
... using a large variety of covariates considered as potential predictors of poor outcome in patients with ...the prognostic score were categorized using predetermined (based on clinical ... Voir le document complet
8
SERPINA1 Z allele is associated with cystic fibrosis liver disease
... Overall, 3% of the CF patients carried the SERPINA1 Z allele and 13% the S ...similar for patients with severe CFLD (HR = ...significance. With respect to severe CFLD, there were only seven ... Voir le document complet
25
Long-term effects of azithromycin in patients with cystic fibrosis
... to a decreased number of oral antibiotic courses ...first year of azithromycin treatment (T12 - T24 and T24 - T36), the number of exacerbations increased again ...third year) to reach levels similar ... Voir le document complet
30
Pandoraea pulmonicola chronic colonization in a cystic fibrosis patient, France
... misidentification with bacteria of the genus Burkholderia and Ralstonia has been reported ...outcomes for patients colonized with these bacteria especially in the context of lung transplantation ... Voir le document complet
4
The Airway Microbiota in Cystic Fibrosis: A Complex Fungal and Bacterial Community-Implications for Therapeutic Management
... associated with co-colonization of fungi and bacteria [5,22,49,80], we coupled fungal analysis to the characterization of bacterial flora in sputum samples from CF adults using the pyrosequencing ...lacks ... Voir le document complet
14
Determinants of mortality for adults with cystic fibrosis admitted in Intensive Care Unit: a multicenter study.
... patients with CF predicts a shift in patients with life-threatening complications from pediatric ICU to adult ICU ...questioned for adult CF patients with advanced lung ...patients ... Voir le document complet
11
Cystic fibrosis respiratory tract salt concentration An Exploratory Cohort Study
... accordance with those measured in vivo in CF pig and mouse animal models and in vitro in human bronchial epithelium ...correlate with environmental salt concentrations, [14] our data provide grounds ... Voir le document complet
5
Should a neck dissection be performed on patients with cN0 adenoid cystic carcinoma? A REFCOR propensity score matching study
... Darrouzet, H. De Kermadec, P. Dessi, B. Devauchelle, L. Digue, G. Dolivet, F. Dubrulle, S. Duflo, X. Dufour, C. Even, S. Faivre, N. Fakhry, F. R. Ferrand, C. Fer- ron, F. Floret, L. de Gabory, R. Garrel, L. Geoffrois, L. ... Voir le document complet
9
A gacS deletion in Pseudomonas aeruginosa cystic fibrosis isolate CHA shapes its virulence
... in a CHADretS background (Figure 6C). Complemen- tation of CHA with gacS gene affected the phenotype ...nosins A and B, whose biological relevance is still not known ...pigments with redox ... Voir le document complet
11
International prognostic score for asymptomatic early-stage chronic lymphocytic leukemia
... Binet A validation ...associated with TTFT in more than 50% of the validation cohorts were used to con- struct the final ...assigned a weighted-risk score to each factor based on the regression ... Voir le document complet
11
AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations
... CF. For example, CF patients demonstrate increased activation of RAS in response to salt deprivation that is thought to compensate for salt depletion and prevent dehydration [ 4 ...associated with ... Voir le document complet
9
Translating the genetics of cystic fibrosis to personalized medicine
... associated with stem cell therapy offer attractive ...at a specific site of interest and allow genome modifications of the gene ...gRNA for DNA targeting is cheap and easy to design and ...homozygous ... Voir le document complet
24
Cystic fibrosis is associated with a defect in apical receptor-mediated endocytosis in mouse and human kidney.
... Center for Human Genetics, University of Leuven, Leuven, Belgium; and ‡‡ Departments of Biochemistry/Cell Biology, Erasmus University Medical Center, Rotterdam, The ... Voir le document complet
12
High-flow nasal oxygen versus noninvasive ventilation in adult patients with cystic fibrosis: a randomized crossover physiological study
... conditions for these measurements The lack of effect of diaphrag- matic work might probably be explained by the rela- tively normalized (approximately 30%) TFdi in these patients at baseline [ 31 , 32 ] had been ... Voir le document complet
10
Emotional distress and family factors as predictors of quality of life in Children with Cystic Fibrosis
... improve patients’ health but also to enhance their quality of life (QOL) . Accordingly, QOL of school-aged children with CF is relatively under- investigated. • The role of family contextual variables has received ... Voir le document complet
1
Numerical and experimental investigation of mucociliary clearance breakdown in cystic fibrosis
... compatible with the cilia beating cycle [24, 27, 51, ...is a one-way fluid- structure interaction. This assumption is valid only for early stage of the sickness or for stabilized patients, ... Voir le document complet
11
Cystic fibrosis transmembrane conductance regulator dysfunction in platelets drives lung hyperinflammation
... μL with 3 μM CFTR inh -172 or 3 μM SKF-96365 for 15 minutes before stimulation with ...throughout a single ...on a LSRII/Fortessa flow cytom- eter (BD ...incubated ... Voir le document complet
15
Highly Diversified Pandoraea pulmonicola Population during Chronic Colonization in Cystic Fibrosis
... support for resistance and whether resistance is innate or acquired in this genus are still ...associated with fitness cost impacting various phenotypic traits including growth rate, virulence, and being ... Voir le document complet
10
Small Hsps as Therapeutic Targets of Cystic Fibrosis Transmembrane Conductance Regulator Protein
... that a large number of cytoplasmic and ER luminal chaperones, and among them many constitutively expressed Hsps, are essential for CFTR ...biogenesis. For example, some of the high molecular weight ... Voir le document complet
16
Preliminary results of the Quality of Life Systemic Inventory for children in Pediatric Cystic Fibrosis: A tool for clinical interventions?
... tool for clinical interventions? Touchèque, ...including cystic fibrosis, as longevity has increased and medical research has progressed (Abbott & Gee, 2003; Gee, Abbott, Conway, Etherington ... Voir le document complet
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